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Water-dispersed fluorescent silicon nanodots as probes for fluorometric determination of picric acid via energy transfer

DOI:10.1007/s00604-018-3135-5 期刊:Microchimica Acta 出版年份:2019 更新时间:2025-09-04 15:30:14
摘要: Water-dispersed fluorescent silicon nanodots (SiNDs) were synthesized by a one-pot hydrothermal method starting from tetraethyl orthosilicate (TEOS) as silicon source and trisodium citrate as reducing reagent. The method is simple and convenient. The SiNDs, with excitation/emission peaks at 347/440 nm and with fluorescence quantum yield of 18% are shown to be viable fluorescent probes for picric acid (PA). The SiNDs strongly bind PA, and their blue fluorescence is quenched. The distance between the donor and acceptor (R0 value) is calculated from fluorescence data to be 2.1 nm. A fluorometric method was worked out that has a linear response in the 8 nM to 50 μM PA concentration range and a 0.92 nM limit of detection. The method has a fast response (2 min) and is well selective over other nitroaromatic compounds and metal ions. The average recoveries from spiked lake water samples ranged between 98.4 and 100.8%.
作者: Wenjing Qi,Hongkun He,Yuling Fu,Maoyu Zhao,Lin Qi,Lianzhe Hu,Chun Liu,Rong Li
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Investigating the use of water-dispersed fluorescent silicon nanodots (SiNDs) as probes for the fluorometric determination of picric acid (PA) via energy transfer.

Water-dispersed fluorescent SiNDs were synthesized by a one-pot hydrothermal strategy using tetraethyl orthosilicate (TEOS) as silicon source and trisodium citrate as reducing reagent. It not only supplies a simple and convenient method to synthesize fluorescent SiNDs, but also develops a novel fluorometric method for PA analysis. Since the fluorometric method possess the advantages of high sensitivity, good selectivity and fast response, it paves an efficient and wide way for the application of fluorescent SiNDs and energy transfer principles in environment analysis. However, it still needs great efforts to synthesize fluorescent SiNDs and makes fluorescence overlap of 100% quantum yield with donors.

The need for working in the UV makes the probe prone to interferences by biomatter. Blood, serum, cells, marine water, waste waters etc. always display strong background UV absorption and fluorescence. The UV light used for fluorescence excitation will be screened off by UV absorbers and this will weaken the signal. The same is true for emitted UV fluorescence which will be screened off. This limitation needs the pretreatment before real sample analysis.

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